BACKGROUND OF THE INVENTION
FIELD OF THE INVENTION
[0001] The present invention relates to thermosensitive recording materials having excellent
thermal response and having minimized tailings of foreign matters adhered to a thermal
head.
DISCUSSION ON RELATED ART
[0002] Thermosensitive recording materials are generally composed of a support having provided
thereon a thermosensitive recording layer containing as major constituents an ordinarily
colorless or slightly colored dye precursor and an electron receptive developer. Upon
being heated by means of a thermal head, thermal pen or laser beam, the dye precursor
instantaneously reacts with the developer to form a recorded image, as disclosed in
Japanese Patent Examined Publication Nos. 43-4160, 45-14039, etc. Because of the advantages
of relatively simple design of devices, easy maintenance and making no noise, the
recording devices employing such thermosensitive recording materials are being used
in a wide field including recording instruments for measurements, facsimiles, printers,
terminal devices for computers, labels, and automatic vending machines for railroad
tickets and the like. Particularly in the field of facsimiles, demand for thermal
sensitive mode has been greatly increasing and the performance of facsimiles has becoming
high speed due to reduction in transmission costs. Facsimiles have reduced the cost
and minimized the energy consumption. In response to such high speed and low energy
performance required for facsimiles, high sensitivity has been demanded for thermosensitive
recording materials. On the other hand, a dot density of thermal head was generally
8 lines/mm but has recently become a density as high as 16 lines/mm. In addition,
a dot area has become small and, demands for printing small-sized characters in high
image quality or printing characters with density gradation by Dither method have
been increasing. Thus, good printability, namely, to obtain images faithfully reproduced
from dots on a head has been much more demanded than ever.
[0003] Attempting to satisfy these requirements, adhesion between a recording sheet and
a thermal head was improved by supercalendering to a strong degree but such a treatment
resulted in defects of decreasing whiteness, i.e., so called background stain, and
the like.
[0004] It is proposed in Japanese Patent Application KOKAI (Laid-Open) No. 56-27394 to provide
an undercoat layer between a thermosensitive layer and the base paper. By the provision
of an undercoat layer, high density images can be obtained in a small energy without
any violent supercalendering and higher density can be achieved than before. It is
believed that the provision of this undercoat layer would be effective for rendering
the surface of a thermosensitive layer after coated smooth by filling up unevenness
of a support to provide a smooth surface.
[0005] As described above, by the provision of undercoat layer, the higher density recording
has been progressed than before. However, demands for much higher density recording
and more improvement in the dot reproducibility in recent years cannot be coped simply
with the provision of undercoat layer merely aiming at smoothening the surface.
SUMMARY OF THE INVENTION
[0006] An object of the present invention is to provide thermosensitive recording materials
having good thermal response and good dot reproducibility in response to requirements
for higher sensitivity and improving dot reproducibility which could not be solved
by the foregoing techniques as described above.
[0007] The present inventors have discovered that by coating a composition comprising fine
organic hollow particles having a ratio of its wall thickness to its particle diameter
being not greater than 0.15 and an oil-absorbing inorganic pigment as an undercoat
layer provided between a support and a thermosensitive layer and have accomplished
the present invention.
[0008] According to the present invention, there is provided a thermosensitive recording
material comprising a support having provided thereon a thermosensitive recording
layer comprising a dye precursor and a color developer capable of developing a color
of said dye precursor upon heating and an undercoat layer comprising fine organic
hollow particles showing a ratio of its wall thickness to a particle diameter being
not greater than 0.15.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0009] That is, by providing an undercoat layer containing the aforesaid fine organic hollow
particles having a ratio of a wall thickness to a particle diameter being 0.15 or
less, it is effective to form smoother surface by filling up unevenness of the support
like the case of an undercoat layer formed by coating a pigment alone; in addition
to the effect, it is believed that due to heat insulating properties possessed by
hollow particles, thermal energy supplied from a thermal head is prevented from radiating
out of the system and hence, the thermal energy would be acted on the thermosensitive
layer more effectively. It is further believed that adhesion between the surface of
thermosensitive paper and a thermal head would be improved because of elasticity of
the hollow particle layer and therefore, excellent dot reproducibility is exhibited.
However, hollow particles having a ratio of its wall thickness to its particle diameter
of being greater than 0.15 are considered to loose their sufficient heat-insulating
properties and elasticity. Accordingly, the thermosensitive recording material having
excellent thermal response which is the object of the present invention cannot be
obtained.
[0010] The wall thickness of the hollow particles is generally in a range of from 0.5 to
10 µm and hence, the particle diameter of the hollow particles is appropriately chosen
from the range of 0.075 to 1.5 µm.
[0011] Herein, the term particle diameter means an average diameter of the hollow particles.
[0012] The organic hollow particles used in the present invention are desirably those that
are neither distorted nor ruptured by heat upon recording or pressure upon supercalendering,
etc. Specifically, styrene resins, acryl resins or styrene-acryl copolymer resins
are preferably used but the organic hollow particles are not particularly limited
thereto so long as they can meet the above-mentioned requirements.
[0013] It is preferred that the undercoat layer be formed into a dual layer. As a first
layer, an undercoat layer comprising the fine hollow particles described above is
provided and as a second layer, an oil-absorbing inorganic pigment is coated, whereby
more effective results can be obtained.
[0014] In the first layer described above, it is also possible to incorporate other pigments
in such an amount that does not interfere with the effect of the fine hollow particles.
As such a pigment, mention may be made of a pigment ordinarily used for coating paper,
etc., e.g., an organic pigment such as polyethylene, polystyrene, ethylene-vinyl acetate,
urea-formaldehyde resin, etc.; diatomaceous earth, talc, kaolin, calcined kaolin,
calcium carbonate, magnesium carbonate, titanium oxide, zinc oxide, silicon oxide,
aluminum hydroxide, zinc hydroxide, barium sulfate, etc. They may be used singly or
as admixture of two or more. An amount of the pigment described above to be used in
combination is not particularly limited but preferably less than 50 wt% of the amount
of the first layer.
[0015] Further in case that a thermosensitive recording layer is directly provided on the
fine organic hollow particle layer, a color forming component melted by thermal energy
from a thermal head is absorbed into the hollow particle layer and colored images
are shielded, sometimes resulting in rather decreasing image density or adherence
of foreign matters onto the thermal head or sticking upon printing. For these reasons,
it is believed that the provision of the oil-absorbing inorganic pigment layer further
onto the hollow particle layer as the second undercoat layer would not only prevent
those defects but also act to render the surface smoother which was already smoothened
by providing the first undercoat layer.
[0016] As the pigment used for the second undercoat layer of the present invention, those
pigments generally used for coating paper, etc. can be used and are exemplified by
calcium carbonate, kaolin, calcined kaolin, zinc oxide, titanium oxide, aluminum hydroxide,
zinc hydroxide, barium sulfate, silicon oxide, etc. Of these, the pigments showing
an oil absorbing amount of 70 ml/100 g or more, especially calcined kaolin and silicon
oxide are preferred ones.
[0017] The fine organic hollow particles as the first layer in the present invention are
effective when they are coated in a coverage of 1 g/m² or more. However, if the hollow
particles are coated in an excessively large amount, properties as paper are rather
injured than improving that of thermosensitive. For example, as the coated layer is
thickened, the base paper is thinned to make its whole thickness even. This would
result in a problem of flexural rigidity. A coverage of 3 to 15 g/m² is thus preferred.
In order to exhibit the function as the second layer without injuring the effect of
the first layer, a coverage of 1 to 10 g/m² of oil-absorbing inorganic pigment of
the second layer is most preferred. Where a coverage in the second layer is large,
the thermal transfer becomes poor so that the heat insulating properties and elasticity
of the first layer are not sufficiently utilizable in some occasion.
[0018] By providing a thermosensitive layer on the thus provided undercoat layer, desired
properties can be obtained.
[0019] Dye precursors used in the present invention are not particularly limited so long
as they are generally used for pressure-sensitive recording paper to thermosensitive
recording paper. Specific examples include the following dye precursors.
(1) Triarylmethane compounds
[0020] 3,3-bis(p-dimethylaminophenyl)-6-dimethylaminophthalide (Crystal Violet lactone),
3,3-bis(p-dimethylaminophenyl)phthalide, 3-(p-dimethylaminophenyl)-3-(1,2-dimethylindol-3-yl)phthalide,
3-(p-dimethylaminophenyl)-3-(2-methylindol-3-yl)phthalide, 3-(p-dimethylaminophenyl)-3-(2-phenylindol-3-yl)phthalide,
3,3-bis(1,2-dimethyl-indol-3-yl)-5-dimethylaminophthalide, 3,3-bis(1,2-dimethylindol-3-yl)-6-dimethylamino
phthalide, 3,3-bis(9-ethylcarbazol-3-yl)-5-dimethylaminophthalide, 3,3-bis(2-phenylindol-3-yl)-5-dimethylaminophthalide,
3-p-dimethylaminophenyl-3-(1-methylpyrrol-2-yl)-6-dimethylaminophthalide, etc.
(2) Diphenylmethane compounds:
[0021] 4,4′-bis-dimethylaminophenyl benzhydryl benzyl ether, N-halophenyl leuco Auramine,
N-2,4,5-trichlorophenyl leuco Auramine, etc.
(3) Xanthene compounds:
[0022] Rhodamine B anilinolactam, Rhodamine B p-chloroanilinolactam, 3-diethylamino-7-dibenzylaminofluorane,
3-diethylamino-7-octylaminofluorane, 3-diethylamino-7-phenylfluorane, 3-diethylamino-7-chlorofluorane,
, 3-diethylamino-6-chloro-7-methylfluorane, 3-diethylamino-7-(3,4-dichloroanilino)fluorane,
3-diethylamino-7-(2-chloroanilino)fluorane, 3-diethylamino-6-methyl-7-anilinofluorane,
3-(N-ethyl-N-tolyl)amino-6-methyl-7-phenethylfluorane, 3-diethylamino-7-(4-nitroanilino)fluorane,
3-dibutylamino-6-methyl-7-anilinofluorane, 3-(N-methyl-N-propyl)amino-6-methyl-7-anilinofluorane,
3-(N-ethyl-N-isoamyl)amino-6-methyl-7-anilinofluorane, 3-(N-methyl-N-cyclohexyl)amino-6-methyl-7-anilinofluorane,
3-(N-ethyl-N-tetrahydrofuryl)amino-6-methyl-7-anilinofluorane, etc.
(4) Thiazine compounds:
[0023] benzoyl leuco methylene blue, p-nitrobenzoyl leuco methylene blue, etc.
(5) Spiro compounds:
[0024] 3-methyl-spiro-dinaphthopyran, 3-ethyl-spiro-dinaphthopyran, 3,3′-dichloro-spiro-dinaphthopyran,
3-benzyl-spiro-dinaphthopyran, 3-methylnaphtho-(3-methoxybenzo)spiro-pyran, 3-propyl-spiro-benzopyran,
etc.
These dye precursors can be used singly or as admixtures of two ore more.
[0025] As dye developers used in the present invention, electron accepting compounds generally
employed for thermosensitive paper are used; in particular, phenol derivatives, aromatic
carboxylic acid derivatives or metal compounds thereof, N,N′-diarylthiourea derivatives,
etc. are used. Among them, particularly preferred ones are phenol derivatives. Specific
examples are p-phenylphenol, p-hydroxyacetophenone, 4-hydroxy-4′-methyldiphenylsulfone,
4-hydroxy-4′-isopropoxydiphenylsulfone, 4-hydroxy-4′-benzene-sulfonyloxydiphenylsulfone,
1,1-bis(p-hydroxyphenol)propane, 1,1-bis(p-hydroxyphenyl)pentane, 1,1-bis(p-hydroxyphenyl)hexane,
1,1-bis(p-hydroxyphenyl)cyclohexane, 2,2-bis(p-hydroxyphenyl)propane, 2,2-bis(p-hydroxyphenyl)butane,
2,2-bis(p-hydroxyphenyl)hexane, 1,1-bis(p-hydroxyphenyl)-2-ethylhexane, 2,2-bis(3-chloro-4-hydroxyphenyl)propane,
1,1-bis(p-hydroxyphenyl)-1-phenylethane, 1,3-di[2-(p-hydroxyphenyl)-2-propyl] benzene,
1,3-di[2-(3,4-dihydroxyphenyl)-2-propyl]benzene, 1,4-di[2-(p-hydroxyphenyl)-2-propyl]benzene,
4,4′-dihydroxydiphenyl ether, 4,4′-dihydroxydiphenylsulfone, 3,3′-dichloro-4,4′-dihydroxydiphenylsulfone,
3,3′-diallyl-4,4′-dihydroxydiphenylsulfone, 3,3′-dichloro-4,4′-dihydroxydiphenylsulfide,
methyl 2,2-bis(4-hydroxyphenyl)acetate, butyl 2,2-bis(4-hydroxyphenyl) acetate, 4,4′-thiobis(2-t-butyl-5-methylphenol),
bis(3-allyl-4-hydroxyphenyl)sulfone, 4-hydroxy-4′-isopropyloxydiphenylsulfone, 3,4-dihydroxy-4′-methyldiphenylsulfone,
benzyl p-hydroxybenzoate, chlorobenzyl p-hydroxybenzoate, propyl p-hydroxybenzoate,
butyl p-hydroxybenzoate, dimethyl 4-hydroxyphthalate, benzyl gallate, stearyl gallate,
salicylanilide, 5-chlorosalicylanilide, etc.
[0026] In addition, the thermosensitive layer may also contain as pigments diatomaceous
earth, talc, kaolin, calcined kaolin, calcium carbonate, magnesium carbonate, titanium
oxide, zinc oxide, silicon oxide, aluminum hydroxide, urea-formalin resin, etc.; may
further contain waxes such as N-hydroxymethylstearic amide, stearic amide, palmitic
amide, etc.; naphthol derivatives such as 2-benzyloxynaphthalene, etc.; biphenyl derivatives
such as p-benzylbiphenyl, 4-allyloxybiphenyl, etc.; polyether compounds such as 1,2-bis(3-methylphenoxy)ethane,
2,2′-bis(4-methoxyphenoxy)diethyl ether, bis (4-methoxyphenyl) ether, etc.; carbonate
or oxalate diester derivatives such as diphenyl carbonate, dibenzyl oxalate, di(p-fluorobenzyl)
oxalate, etc. for purposes of further improving the sensitivity.
[0027] In addition, there may be incorporated, for purposes of preventing head abrasion,
prevention of sticking, etc., higher fatty acid metal salts such as zinc stearate,
calcium stearate, etc.; waxes such as paraffin, oxidized paraffin, polyethylene, oxidized
polyethylene, stearic amide, castor wax, etc.; dispersing agents such as sodium dioctylsulfosuccinate,
etc.; UV absorbing agents of benzophenone type, benzotriazole type, etc. and further
surface active agents, fluorescent dyes, etc., if necessary and desired.
[0028] In the present invention, as adhesives used for the first undercoat layer, second
undercoat layer and thermosensitive recording layer used in the present invention,
various adhesives generally used are usable. Examples of the adhesives include water
soluble adhesives such as starches, hydroxyethyl cellulose, methyl cellulose, carboxymethyl
cellulose, gelatin, casein, polyvinyl alcohol, modified polyvinyl alcohol, sodium
polyacrylate, acrylic amide/acrylate copolymer, acrylamide/acrylate/methacrylate ternary
copolymer, alkali salts of styrene/maleic anhydride copolymer, alkali salts of ethylene/maleic
anhydride copolymer, etc.; latexes such as polyvinyl acetate, polyurethane, polyacrylates,
styrene/butadiene copolymer, acrylonitrile/butadiene copolymer, methyl acrylate/butadiene
copolymer, ethylene/vinyl acetate copolymer, etc. As the support used in the present
invention, paper is mainly used. Non-woven cloth, a plastic film, synthetic paper,
metal foil and the like or a composite sheet obtained by combining them may optionally
be employed.
EXAMPLES
[0029] Next, the present invention will be described in more detail by referring to the
examples.
[0030] Parts and % shown below are all by weight. Numeral values representing coated amounts
or coverages are dry weights, unless indicated.
Example 1
(1) Preparation of Suspension A (coating liquid for the first layer)
[0031] A mixture having the following composition was stirred to prepare a coating liquid
for the first layer.

(2) Preparation of Suspension B (coating liquid for the second layer)
[0032] A mixture having the following composition was stirred to prepare a coating liquid
for the second layer.
ANSILEX (calcined kaolin, made by Engelhardt Co., Ltd.) |
100 parts |
Styrene-butadiene copolymer latex (50% aqueous dispersion) |
24 parts |
|
MS 4600 (phosphated starch, 10% aqueous solution, made by Nippon Shokuhin K.K.) |
60 parts |
Water |
52 parts |
(3) Preparation of Thermosensitive Suspension
[0033] A mixture having the following composition was ground into a mean grain diameter
of about 1 µm with a sand grinder to prepare [Suspension C] and [Suspension D], respectively.
[Suspension C] |
3-dibutylamino-6-methyl-7-anilinofluorane |
40 parts |
10% Polyvinyl alcohol aqueous solution |
20 parts |
Water |
40 parts |
[Suspension D] |
Bisphenol A |
50 parts |
Benzyloxynaphthalene |
50 parts |
10% Polyvinyl alcohol aqueous solution |
50 parts |
Water |
100 parts |
[0034] Then, a thermosensitive suspension was prepared in the following formulation, using
the thus prepared [Suspension C] and [Suspension D].
[Suspension C] |
50 parts |
[Suspension D] |
250 parts |
Zinc stearate (40% dispersion) |
25 parts |
10% Polyvinyl alcohol aqueous solution |
216 parts |
Calcium carbonate |
50 parts |
Water |
417 parts |
[0035] Each of the thus prepared coating suspensions was coated onto a base paper weighing
40 g/m² in the following coverages with a Mayor bar to prepare a thermosensitive recording
material.
First layer |
8 |
g/m² |
Second layer |
3 |
g/m² |
Thermosensitive layer |
5.5 |
g/m² |
Example 2
[0036] After the suspension for the first layer was coated in a coverage of 8 g/m² in Example
1, the suspension for thermosensitive layer was directly coated thereon in a manner
similar to Example 1, without providing the suspension for the second layer. Thus,
a thermosensitive recording material was prepared.
Example 3
[0037] A thermosensitive recording material was prepared in a manner similar to Example
1 except that 100 parts of Ultra White 90 (kaolin for the purpose of coating, made
the Engelhardt Co.) were used instead of 100 parts of ANSILEX in the preparation of
Suspension B (coating liquid for the second layer) in Example 1.
Comparative Example 1
[0038] A thermosensitive recording material for the comparative study was prepared in a
manner similar to Example 1 except that a mixture having the following composition
was prepared and coated in a coverage of 8 g/m² as the coating liquid for the first
layer, instead of [Suspension A] in Example 1.

Comparative Example 2
[0039] A thermosensitive recording material for the comparative study was prepared by directly
coating the coating liquid for the second layer onto base paper in a coverage of 8
g/m², without coating the coating liquid for the first layer, both prepared in Example
1, and coating a thermosensitive coating liquid thereon in a coverage of 5.5 g/m².
Comparative Example 3
[0040] A thermosensitive recording material for the comparative study was prepared in a
manner similar to Example 1 except that the thermosensitive coating liquid was directly
coated onto a base paper weighing 40 g/m², in a coverage of 5.5 g/m², without coating
the coating liquid for the first layer nor that for the second layer, both prepared
in Example 1.
[0041] The thus prepared thermosensitive recording materials were treated by supercalendering
so as to have them complied with a Beck's degree of smoothness varied between 400
and 500 seconds. And these materials were compared with respect to recording density,
printability and degree of adhering tailings or foreign matters using a GIII facsimile
test machine. A test machine was (TH-PMD) manufactured by Okura Electric Co., Ltd.
Printing was performed using a thermal head showing its dot density of 8 dots/mm and
its head resistance of 185 ohm, at a head voltage of 15 V, for its load time of 0.08
ms and 0.10 ms. Recording density was measured with Macbeth RD-918 reflection densitometer.
These results are shown in Table 1.
Table 1
|
|
Sensitivity |
|
|
|
|
0.08 ms |
0.10 ms |
Printability |
Tailings |
Example |
1 |
0.55 |
1.05 |
o |
o |
|
2 |
0.52 |
0.88 |
o - Δ |
o - Δ |
|
3 |
0.51 |
0.91 |
o |
o - Δ |
Comparative Example |
1 |
0.40 |
0.79 |
Δ |
o |
|
2 |
0.33 |
0.71 |
Δ |
o |
|
3 |
0.15 |
0.44 |
x |
x |
o : Good |
o-Δ : Relatively good |
Δ : No good |
x : Bad |
[0042] As is evident from the results of Table 1, the thermosensitive recording materials
of the present invention, wherein the thermosensitive layer was coated onto the undercoat
layer bearing a coated layer composed of fine organic hollow particles having a ratio
of its wall thickness to its particle diameter being 0.15 or less, were excellent
in thermal response, as compared to conventional thermosensitive recording materials
and could achieve improved sensitivity and improved dot reproducibility. It was further
noted that by providing the coated layer composed of oil-absorbing inorganic pigments
between the hollow particle layer and the thermosensitive layer, improved sensitivity
and improved dot reproducibility could be achieved, without increasing foreign matters
adhered to the head.
[0043] While the invention has been described in detail and with reference to specific embodiments
thereof, it is apparent to one skilled in the art that various changes and modifications
can be made therein without departing from the spirit and the scope of the present
invention.